Autosomal recessive hereditary disorder	Congenital malformation of the eyebrow	Developmental hereditary disorder	Diprosopus	Hereditary disorder of the visual system	Multiple malformation syndrome with facial-limb defects as major feature	Syndactyly of fingers	Syndactyly of toes
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Duplication of eyebrow and syndactyly syndrome (disorder)
	Duplication of eyebrow and syndactyly syndrome
	Eyebrow duplication syndactyly syndrome
	Syndrome with characteristics of partial duplication of the eyebrows and syndactyly of the fingers and toes. It has been described in three patients (a brother and sister and an isolated case). Skin hyperelasticity, hypertrichosis and long eyelashes and abnormal periorbital wrinkling were also reported in some of the patients. Transmission is autosomal recessive.
	syndroom van wenkbrauwduplicatie en syndactylie

Id	733070005
Status	Primitive

Associated morphology	Double structure
Finding site	Eyebrow structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Congenital abnormal fusion
Finding site	Toe structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Congenital abnormal fusion
Finding site	Finger structure
Occurrence	Congenital
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q18.8
Rule	TRUE
Advice	ALWAYS Q18.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified

Target	Q70.1
Rule	TRUE
Advice	ALWAYS Q70.1
Correlation	SNOMED CT source code to target map code correlation not specified

Target	Q70.3
Rule	TRUE
Advice	ALWAYS Q70.3
Correlation	SNOMED CT source code to target map code correlation not specified